Taiwan FDA registration 7153234e673c568ea0c1e59ae8bf92e5
"Jingxuan" suction aid (unsterilized)
TW: “敬煇”吸藥輔助器(未滅菌)
Taiwan·Risk Class 1·TAIEX CO., LTD.·Registered Apr 08, 2008 – Apr 08, 2013CancelledRegistration details
- Analysis ID
- 7153234e673c568ea0c1e59ae8bf92e5
Company information
- Manufacturer
- TAIEX CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIEX CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5640 非呼吸用醫藥噴霧器(atomizer)
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 08, 2008
- Expiry Date
- Apr 08, 2013
- Cancellation Date
- Nov 19, 2010
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Jingxuan" suction aid (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7153234e673c568ea0c1e59ae8bf92e5 and manufactured by TAIEX CO., LTD.. The authorized representative in Taiwan is TAIEX CO., LTD..
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